WO1998001483A1 - Procede pour fabriquer des (co)polymeres de cyclo-olefines destines a des memoires de donnees optiques - Google Patents

Procede pour fabriquer des (co)polymeres de cyclo-olefines destines a des memoires de donnees optiques Download PDF

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Publication number
WO1998001483A1
WO1998001483A1 PCT/EP1997/003459 EP9703459W WO9801483A1 WO 1998001483 A1 WO1998001483 A1 WO 1998001483A1 EP 9703459 W EP9703459 W EP 9703459W WO 9801483 A1 WO9801483 A1 WO 9801483A1
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Prior art keywords
group
compounds
acceptor
donor
charge
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PCT/EP1997/003459
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German (de)
English (en)
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WO1998001483A9 (fr
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Karl-Heinz Aleksander Ostoja Starzewski
Warren Mark Kelly
Andreas Stumpf
Claudia Schmid
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Bayer Aktiengesellschaft
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Priority claimed from DE19627064A external-priority patent/DE19627064C2/de
Priority claimed from DE19714058A external-priority patent/DE19714058A1/de
Application filed by Bayer Aktiengesellschaft filed Critical Bayer Aktiengesellschaft
Priority to JP10504738A priority Critical patent/JP2000514116A/ja
Priority to DE59702429T priority patent/DE59702429D1/de
Priority to AU36927/97A priority patent/AU3692797A/en
Priority to AT97933647T priority patent/ATE196771T1/de
Priority to EP97933647A priority patent/EP0909285B1/fr
Priority to US09/214,206 priority patent/US6232413B1/en
Publication of WO1998001483A1 publication Critical patent/WO1998001483A1/fr
Publication of WO1998001483A9 publication Critical patent/WO1998001483A9/fr
Priority to NO990015A priority patent/NO990015L/no

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    • C08F4/61922—Component covered by group C08F4/60 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring containing at least two cyclopentadienyl rings, fused or not
    • C08F4/61927—Component covered by group C08F4/60 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring containing at least two cyclopentadienyl rings, fused or not two cyclopentadienyl rings being mutually bridged
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    • C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
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    • C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
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    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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Definitions

  • the present invention relates to the use of ⁇ systems or metallocene compounds in which a transition metal is complexed with two ⁇ systems, in particular with aromatic ⁇ systems, such as anionic cyclopentadienyl ligands (carbanions), and the two Systems are reversibly connected to one another by at least one bridge of a donor and an acceptor, as organometallic catalysts in a process for the preparation of cycloolefin (co) polymers for use in optical data storage by (co) -
  • Cycloolefin (co) polymers are characterized by many advantageous properties, such as high transparency for use in the field of optical data storage, in particular for compact discs (CD) with a high storage density. They also have good thermal resistance, aging resistance, chemical resistance, solvent resistance, low water absorption, high scratch resistance, low light birefringence and high softening temperatures
  • Linking group represents a (substituted) methylene group or ethylene group, a silylene group, a substituted silyien group, a substituted germylene group or a substituted phosphine group.
  • the bridged metallocenes are provided as polymerization catalysts for olefins.
  • catalysts can be prepared from bridged ⁇ complex compounds and in particular from metallocene compounds in which the bridging of the two ⁇ systems is produced by one, two or three reversible donor-acceptor bonds, in which a coordinative or so-called dative bond is formed between the donor atom and the acceptor atom, which is at least formally superimposed on an ionic bond and in which one of the donor or acceptor atoms can be part of the associated ⁇ system.
  • the ⁇ systems to be used according to the invention can also be used in the non-bridged state, for example metallocenes can therefore be identified by a double arrow and the formula parts (Ia) and (Ib) or (Xllla) and ( Xlllb) to encompass both conditions
  • the invention accordingly relates to a process for the preparation of cycloolefin
  • (Co) polymers for use in optical data storage by (co) polymers of monomers from the group of cyclic olefins, the ⁇ -olefins with 2 or more carbon atoms and optionally conjugated or non-conjugated diolefins in the gas, bulk, solution or slurry phase at -78 to + 200 ° C and 0.5-70 bar in the presence of organometallic catalysts that can be activated by cocatalysts , which is characterized in that the organometallic catalysts are metallocene compounds of the formula
  • Cpl and CpII represent two identical or different carbanions with a cyclopentadienyl-containing structure, in which one to all H atoms by identical or different radicals from the group of linear or branched C ] -C20 "Al yl, the 1-fold can be completely substituted by halogen, 1-3 times by phenyl and 1-3 times by vinyl, Cg-C ⁇ aryl,
  • Halogenaryl with 6 to 12C atoms organometallic substituents, such as silyl, trimethylsilyl, ferrocenyl, and can be substituted 1 or 2 times by D and A,
  • D denotes a donor atom which can additionally carry substituents and which has at least one lone pair of electrons in its respective bond state
  • A denotes an acceptor atom which can additionally carry substituents and which has an electron pair gap in its respective bond state, where D and A are linked by a reversible coordinative bond in such a way that the donor group assumes a positive (partial) charge and the acceptor group a negative (partial) charge,
  • Periodic table of the elements including the lanthanides and actinides,
  • X represents an anion equivalent
  • ⁇ l and ⁇ ll represent differently charged or electrically neutral ⁇ systems, which can be condensed once or twice with unsaturated or saturated five or six rings,
  • D denotes a donor atom which is a substituent of ⁇ l or part of the ⁇ system of ⁇ l and which has at least one lone pair of electrons in its respective bond state
  • A denotes an acceptor atom which is a substituent of ⁇ ll or part of the ⁇ system of ⁇ ll and which has an electron pair gap in its respective bond state
  • D and A are linked by a reversible coordinative bond in such a way that the donor group takes on a positive (partial) charge and the acceptor group takes on a negative (partial) charge, and at least one of D and A is part of the respective ⁇ system,
  • each ⁇ system or each fused ring system can contain one or more D or A or D and A and
  • Organometallic substituents such as silyl, trimethylsilyl, ferrocenyl and mono- or disubstituted by D and A, so that the reversible coordinative D— »A bond (i) between D and A, both parts of the respective ⁇ system or of the condensed ring system, or (ii) of which D or A is part of the ⁇ system or of the condensed ring system and the other substituent of the uncondensed ⁇ system or of the condensed ring system is (are) formed,
  • ⁇ systems according to the invention are substituted and unsubstituted ethylene, allyl, pentadienyl, benzyl, butadiene, benzene, the cyclopentadienyl anion and the species resulting from replacement of at least one C atom by a heteroatom.
  • the cyclic ones are preferred.
  • the type of coordination of such ligands ( ⁇ systems) to the metal can be of the ⁇ type or of the ⁇ type.
  • Such metallocene compounds of the formula (I) to be used according to the invention can be prepared by either using a compound of the formulas (II) and (III)
  • CpIII and CpIV represent two identical or different uncharged parts of the molecule with a structure containing cyclopentadiene, but are otherwise the same as Cpl and CpII,
  • M ' represents a cation equivalent of an (earth) alkali metal or Tl
  • E and F independently of one another represent one of the elements Si, Ge or Sn and
  • X can be of E (R 1 R 2 R 3) and F (R4R5R6) hydrogen while still in place in the formulas (VIII), (IX), (X) and in this case X may also represent an amide anion of the type R2N ⁇ or Carbanion of the type R3C ⁇ or an alcoholate anion of the type
  • RO ⁇ can be, and it is also possible to react compounds of the formulas (II) or (VIII) directly in the presence of compounds of the formulas (V) or (IX) with a transition metal compound of the formula (VII).
  • Two anions X can also be joined to form a dianion, optionally with the interposition of a mono- or polyatomic bridge.
  • Ether's ROE (R 1 R 2 R 3 ) or ROF (R 4 R 5 R 6 ), in which the organic radicals R are identical or different and independently of one another C 1 -C 20 -alkyl, are substituted or unsubstituted allyl, benzyl or hydrogen.
  • Examples of escaping amine or hydrocarbon, ether, silane, stannane or German are, for example, dimethylamine, diethylamine, di- (n-propyl) amine, di- (isopropyl) amine, di- (tertiary-butyl) amine, tertiary butylamine, Cyclohexylamine, aniline, methylphenylamine, di- (allyl) amine or methane, toluene, trimethylsilylamine, trimethylsilyl ether, tetramethylsilane and the like.
  • Open-chain ⁇ -complex compounds are produced according to the processes known in the art with the incorporation of donor and acceptor groups
  • the metallocene compounds or the ⁇ -complex compounds as catalysts in an amount of 101 to 10 ⁇ 2 mol of all monomers per mol of metallocene or ⁇ -complex compounds are used and it is also possible to work in the presence of Lewis acids, Bronstedt acids or Pearson acids or additionally in the presence of Lewis bases
  • Such Lewis acids are, for example, boranes or alanes, such as aluminum alkyls, aluminum halides, aluminum alcoholates, boron halides, boron halides, boric acid esters or boron or aluminum compounds which contain both halide and alkyl or aryl or alcoholate substituents, and Mixtures thereof or the triphenylmethyl cation.
  • Particularly preferred are aluminoxanes or mixtures of aluminum-containing Lewis acids with water. According to current knowledge, all acids act as ionizing agents which form a metallocenium cation which is charge-compensated by a bulky, poorly coordinating anion
  • reaction products of such ionizing agents with metallocene compounds of the formula (I) or (XIII) can also be used. They can be described by the formulas (XIa) to (Xld) or
  • metallocene compounds (I) or (XIII) which can be used according to the invention can be present in monomeric, dimeric or oligomeric form
  • sulfonates such as tosylate or triflate, tetrafluoroborates, hexafluorophosphates or
  • metallocene compounds can act as highly effective polymerization catalysts even in the absence of aluminoxane. This is particularly the case when an X- Ligand represents an alkyl group, allyl or benzyl.
  • metallocene complexes with bulky anions in combination with aluminum alkyls, such as (CH 3 ) 3 A1, C2H5) 3 A1, (n- / i-propyl) 3 Al , (n- / t-Butyl) Al, (i-butyl) Al, the isomeric pentyl, hexyl or octyl aluminum alkyls, or lithium alkyls, such as methyl-Li, benzyl-Li, butyl-Li or the corresponding Mg to use organic compounds such as Grignard compounds or Zn organyls.
  • aluminum alkyls such as (CH 3 ) 3 A1, C2H5) 3 A1, (n- / i-propyl) 3 Al , (n- / t-Butyl) Al, (i-butyl) Al
  • the isomeric pentyl, hexyl or octyl aluminum alkyls or lithium alkyls
  • metal alkyls transfer alkyl groups to the central metal on the one hand, and on the other hand they catch water or catalyst poisons from the reaction medium or monomer in the polymerization reaction
  • Ions from metal alkyls of the type described can also advantageously be used in combination with aluminum oxane cocatalysts, for example in order to lower the required amount of aluminoxane.
  • Examples of boron compounds in whose use such anions are introduced are , , ,
  • Tri (t-butyl) ammonium tetraphenylborate N, N-dimethylanilinium tetraphenylborate
  • Dialkylammonium salts such as: di- (i-propyl) ammonium tetrakis (pentafluorophenyl) borate and
  • Tri-substituted phosphonium salts such as:
  • Triphenylphosphonium tetrakis (pentafluorophenyl) borate Triphenylphosphonium tetrakis (pentafluorophenyl) borate
  • the first and the second carbanion Cpl and CpII with a cyclopentadienyl skeleton can be the same or different.
  • the cyclopentadienyl skeleton can be, for example, one from the group of cyclopentadiene, substituted cyclopentadiene, indene, substituted indene, fluorene and substituted fluorene.
  • the substituents are 1 to 4 per cyclopentadiene or fused benzene ring. These substituents can be C] -C20-alkyl, such as methyl, ethyl, propyl, isopropyl, butyl or iso-
  • Fluorine, chlorine, bromophenyl, naphthyl or biphenylyl, triorganylsilyl, such as trimethylsilyl (TMS), ferrocenyl and D or A, as defined above, can also be partially or completely hydrogenated aromatic rings, so that only the double bond exists remains, in which both the fused ring and the cyclopentadiene ring participate. Can continue
  • Benzene rings as in indene or fluorene, contain one or two further fused benzene rings. Furthermore, the cyclopentadiene or cyclopentadienyl ring and a fused-on benzene ring can together contain another fused benzene ring
  • Such cyclopentadiene skeletons are excellent ligands for transition metals in the form of their anions, with each cyclopentadienyl carbanion a substituted form compensates for a positive charge of the central metal in the complex.
  • carbanions are: cyclopentadienyl, methyl-cyclopentadienyl, 1, 2-dimethyl-cyclopentadienyl, 1, 3-dimethyl-cyclopentadienyl, indenyl, phenylindenyl, 1,2-diethyl-cyclopentadienyl, tetramethyl-cyclopentadienyl, ethyl-cyclopentadienyl, Butyl-cyclopentadienyl, n-octyl-cyclopentadienyl, ß-
  • Fluorenyls and indenyls N, N-dimethylamino-cyclopentadienyl, dimethylphosphinocyclopentadienyl, methoxy-cyclopentadienyl, dimethylboranyl-cyclopentadienyl, (N, N-dimethylaminomethyl) cyclopentadienyl.
  • donor-acceptor bonds can be formed if additional D and / or A are present as substituents of the respective cyclopentadiene systems or as substituents or parts of the ⁇ system. All donor-acceptor bonds are characterized by their reversibility shown above. In the case of several D or A, they can assume different positions.
  • the invention accordingly comprises both the bridged molecular states (Ia) and (Xllla) and the unbridged states (Ib) and (Xfflb).
  • the number of D groups can be the same or different from the number of A groups.
  • Cpl and CpII or ⁇ l or ⁇ ll are preferably linked via only one donor-acceptor bridge.
  • covalent bridges can also be present.
  • the D / A bridges increase the stereorigidity and the thermostability of the catalyst.
  • sequence polymers for copolymers with different chemical compositions become accessible.
  • the ⁇ complex compounds are also characterized by the presence of at least one coordinative bond between donor atom (s) D and acceptor atom (s) A.
  • D and A can be substituents of their respective ⁇ systems ⁇ l or ⁇ ll or part of ⁇ System, but at least one of D and A is always part of the ⁇ system.
  • the ⁇ system is understood here to mean the entire ⁇ system, which may be condensed once or twice. The following embodiments result from this:
  • D is part of the ⁇ system, A is a substituent of the ⁇ system; D is a substituent of the ⁇ system, A is part of the ⁇ system; D and A are parts of their respective ⁇ systems.
  • Examples include the following heterocyclic ring systems in which D or A are part of the ring system:
  • Important heterocyclic ring systems are those designated (a), (b), (c), (d), (g), (m), (n) and (o); particularly important are those designated by (a), (b), (c) and (m).
  • the ring system is 3-, 4-, 5-, 6-, 7- or 8-membered with or without electrical charge, which further substitutes in the manner indicated and / or can be condensed.
  • 5- and 6-membered ring systems are preferred.
  • the negatively charged cyclopentadienyl system is particularly preferred.
  • the first and the second ⁇ system ⁇ l and ⁇ ll if it is designed as a ring system, can correspond to Cpl or CpII if one of D and A is a substituent of the ring system.
  • Particularly suitable donor groups are those in which the donor atom D is an element of the 5th, 6th or 7th, preferably the 5th or 6th main group of the Periodic Table of the Elements (Mendeleev) and has at least one lone pair of electrons and where the donor atom is in the case of elements of the 5th main group in a binding state with substituents and can be in such a case in the case of elements of the 6th main group; Donor atoms of the 7th main group have no substituents.
  • Acceptor groups are primarily those whose acceptor atom A is an element from the 3rd main group of the Periodic Table of the Elements (Mendeljew), such as boron, aluminum, gallium, indium and thallium, is in a bonded state with substituents and has an electron gap
  • D and A are linked by a coordinative bond, where D assumes a positive (partial) charge and A a negative (partial) charge
  • the coordinative bond D -> A is established between the donor atom D and the acceptor atom A.
  • the donor group means the unit from the donor atom D, the optionally present substituents and the electron pairs present, accordingly the acceptor group means the unit from the acceptor atom A, the
  • the bond between the donor atom or the acceptor atom and the cyclopentadienyl-containing carbanion can be interrupted by spacer groups in the sense of D-spacer-Cp or A-spacer-Cp.
  • D and A can independently of one another sit on the cyclopentadiene (yl) ring or a fused-on benzene ring or another substituent of Cpl or CpII or ⁇ l or ⁇ ll. In the case of several D or A, they can assume different positions.
  • Acceptor atoms B, Al, Ga, In and Tl are, for example: C j -Ci2 (cyclo) alkyl, such as methyl, ethyl, propyl, i-propyl, cyclopropyl, butyl, i-butyl, tert-butyl, cyclobutyl, pentyl , Neopentyl, cyclopentyl, hexyl, cyclohexyl, the isomeric heptyls, octyls, nonyls, decyls, undecyls, dodecyls; the corresponding C j -C ⁇ alkoxy groups; Vinyl, butenyl, allyl; Cg-C ⁇ aryl, such as phenyl, naphthyl or biphenylyl,
  • Benzyl which can be substituted by halogen, 1 or 2 Cj-C i-alkyl groups, C] -C4-alkoxy groups, nitro or haloalkyl groups, Ci-Cö-alkyl-carboxy, Ci-Cg-alkyl-carbonyl or cyano (e.g. perfluorophenyl , m, m'-bis (trifluoromethyl) phenyl and analogous substituents familiar to the person skilled in the art); analog aryloxy groups; Indenyl; Halogen, such as F, Cl, Br and I, 1-thienyl, disubstituted amino, such as (C j -
  • Silyl groups which are bonded to the donor atom or the acceptor atom via -CH2-, for example (CH 3 ) 3 SiCH2-, (C] -Ci 2-alkyl) (phenyl) amino, (-C 1 -Ci2-alkylphenyl) 2amino , Cß-C ⁇ aryloxy with the above aryl groups, Ci -Cg-perfluoroalkyl, perfluorophenyl.
  • Preferred substituents are: -CSS Ci-alkyl, C5-C6 cycloalkyl, phenyl, tolyl, C] -CG-alkoxy, C6-C ⁇ 2 aryloxy, vinyl, allyl, benzyl, perfluorophenyl, F, Cl, Br, di- (-C -C6 alkyl) amino, diphenylamino.
  • -C (CH 3 ) O, -OSi (CH 3 ) 3 , -OSi (CH 3 ) 2 -t-butyl, in which N and P each carry one lone pair and O and S each carry two lone pairs and where in the last two examples, the double-bonded oxygen is bonded via a spacer group, and systems such as the pyrrolidone ring, the ring members other than N likewise acting as spacers
  • Acceptor groups are those in which there is an electron pair gap on B, Al, Ga, In or Tl, preferably B, Al, examples include (CH) 2B-, (C 2 H 5 ) 2 B-, H 2 B -, (C 6 H 5 ) 2 B-, (CH 3 ) (C 6 H 5 ) B-, (vinyl) 2 B-, (benzyl) 2 B-, C1 2 B-, (CH 3 O) 2 B-, C1 2 A1-, (CH 3 ) AI-, (iC 4 H 9 ) 2 Al-, (C1) (C 2 H 5 ) 2 A1-, (CH 3 ) 2 Ga-,
  • donor and acceptor groups are suitable which contain chiral centers or in which 2 substituents have one with the D or A atom
  • Preferred donor-acceptor bridges between Cpl and CpII are, for example, the following _ _
  • One or both ⁇ systems ⁇ l and ⁇ ll can be present as a heterocycle in the form of the above ring systems (a) to (r).
  • D is preferably an element of the 5th or 6th main group of the Periodic Table of the Elements (Mendeleev);
  • A is preferably boron.
  • hetero- ⁇ systems, in particular heterocycles are:
  • R, R ' H, alkyl, aryl, alkaryl e.g. Methyl, ethyl, t-butyl, phenyl, o, o'-di (i-propyl) phenyl
  • heterocycles are: pyrrolyl, methylpyrrolyl, dimethylpyrrolyl, trimethylpyrrolyl, tetramethylpyrrolyl, t-butylpyrrolyl, di-t-butylpyrrolyl, indolyl, methylindolyl, dimethylindolyl, t-butylindolyl, di-t-butylethylphylylylyltylolyl, tolylylolylyl, tolylolylyl, tri-methyl-tolylolyl, tri-methyl-tolylolyl, tri-methyl-tolylolyl, tryl-methyl , Trimethylphospholyl, phosphaindenyl, dibenzophospholyl (phosphafluorenyl), dibenzopyrrolyl.
  • the two ligand systems ⁇ l and ⁇ ll can be linked by one, two or three donor-acceptor bridges as shown above. This is possible since, according to the invention, the formula (Ia) contains the D - A bridge shown, the ligand systems ⁇ l or ⁇ ll but can carry further D and A as substituents or hetero- ⁇ centers, the number of resulting additional D - »A bridges is
  • the number of D or A substituents on ⁇ l or ⁇ ll can be the same or different.
  • the two ligand systems ⁇ l and ⁇ ll can additionally be covalently linked (examples of covalent bridges are described above as spacer groups) are preferred however, compounds without a covalent bridge, in which ⁇ l and ⁇ ll are linked by only one donor – acceptor bridge
  • M stands for a transition metal from subgroup 3, 4, 5 or 6 of the Periodic Table of the Elements (Mendeleev), including the lanthanides and actimides, examples include Sc, Y, La, Sm, Nd, Lu, Ti, Zr, Hf, Th, V Nb, Ta, Cr
  • one positive charge of the transition metal M is compensated for by a cyclopentadienyl-containing carbanion.
  • Any remaining positive charges on the central atom M are saturated by further, mostly monovalent anions X, two of which the same or different ones can also be linked to one another (dianions * *), for example monovalent or divalent negative residues from the same or different, linear or branched, saturated or unsaturated hydrocarbons, amines, phosphines, thioalcohols, alcohols or phenols.
  • Simple anions such as CR 3 " , NR2", PR2 ", OR", SR " etc.
  • bridge atoms can be saturated or unsaturated hydrocarbon or silane bridges, whereby dianions are formed and the number of bridging atoms can be 0, 1, 2, 3, 4, 5, 6, preferably 0 to 4 bridging atoms, particularly preferably 1 or 2 bridging atoms.
  • the bridge atoms can also carry further KW substituents R. Examples of bridges between the simple anions are -CH2-,
  • Examples of X are: hydride, chloride, methyl, ethyl, phenyl, fluoride, bromide, iodide, the n-propyl radical, the i-propyl radical, the n-butyl radical, the amyl radical, the i-amyl radical, the hexyl radical, the i- Butyl radical, the heptyl radical, the octyl radical, the nonyl radical, the decyl radical, the cetyl radical, methoxy, ethoxy, propoxy, butoxy,
  • Phenoxy dimethylamino, diethylamino, methylethylamino, di-t-butylamino, diphenylamino, diphenylphosphino, dicyclohexylphosphino, dimethylphosphino, methylidene, ethylidene, propylidene, the ethylene glycol dianion.
  • dianinones are 1,4-diphenyl-1,3-butadienediyl, 3-methyl-1,3-pentadienediyl, 1,4-dibenzyl-1,3-butadienediyl, 2,4-hexadienediyl, 1,3- Pentadiendiyl, l, 4-ditolyl-l, 3-butanediene diyl, 1,4-bis (trimethylsilyl-l, 3-butadiene diyl, 1,3-butadiene diyl.
  • 1,4-diphenyl-l, 3 are particularly preferred -butandienediyl, 1,3-pentadienediyl, l, 4-dibenzyl-l, 3-butadienediyl, 2,4-hexandienediyl, 3-methyl-1,3-pentadienediyl, l, 4-ditolyl-l-3-butadienediyl and 1 , 4- bis (trimethylsilyl) -l, 3-butadienediyl
  • dianions are those with heteroatoms, for example of the structure
  • Activation by such voluminous anions is achieved, for example, by reacting the D / A- ⁇ complex compounds, in particular the D / A metallocenes with tris (pentafluorophenyl) borane, triphenylborane, triphenylaluminum, trityl-tetra-kis (pentafluorophenyl) borate or N, N-dialkylphenylammonium tetrakis (pentafluorophenyl) borate or the corresponding phosphonium or sulfonium salts of 1483.
  • the D / A metallocenes with tris (pentafluorophenyl) borane, triphenylborane, triphenylaluminum, trityl-tetra-kis (pentafluorophenyl) borate or N, N-dialkylphenylammonium tetrakis (pentafluoropheny
  • the reaction products obtainable therefrom can be activated with the above-mentioned boranes or borates without prior isolation
  • the index n takes on the value zero, one, two, three or four, preferably zero, one or two, depending on the charge of M.
  • the above-mentioned subgroup metals can, depending on their affiliation to the subgroups, have valences / charges of Assume two to six, preferably two to four, of which two are compensated for by the carbanions of the metallocene compound.
  • Solvents at temperatures from -78 ° C to + 120 ° C, preferably from -40 ° C to + 70 ° C and in a molar ratio of (II) (III) or (IV) (V) or (VI) (VII) or (VHI).
  • Compounds of the formula (II) or (IV) are therefore carbanions with a cyclopentadienyl skeleton or a heterocyclic skeleton which contain 1 to 3 donor groups used for D / A bridging or covalently bonded or incorporated as Jieterocyclic ring members and as counterions to the negative ones Charge of the cyclopentadienyl skeleton have a cation.
  • Compounds of formula (VIII) are uncharged cyclic scaffolds with 1 to 3 donor groups also used for D / A bridging, but with easily removable leaving groups E (RlR 2 R3), such as silyl, germyl or stannyl groups or hydrogen, instead of the ionic ones Groups.
  • the second component for the formation of the metallocene compounds to be used according to the invention namely the compound of the formula (III) or (V) likewise represents a carbanion with a cyclopentadienyl skeleton which is identical to the cyclopentadienyl skeleton of the compound (II) or (IV) or different from him, but carries 1 to 3 acceptor groups instead of the donor groups.
  • compounds of the formula (IX) are uncharged cyclopentadiene skeletons with 1 to 3 acceptor groups and likewise easily removable leaving groups F (R4R5R6)
  • Both starting materials of the manufacturing process namely (II) and (III) or (IV) and (V) or (VI) and (VII) or (VIII) and (III) or (IV) and (IX) or (X) and (VII) react spontaneously when they are put together, with simultaneous formation of the Donor-acceptor group -D— »A- or the complexation of the metal cation M with the emergence of M'X or E (R ! R 2 R 3 ) X or F (R R5R6) X or HX
  • the substituents on D and A have been omitted for the sake of clarity.
  • M ' is a cation equivalent of an (earth) alkali metal, such as Li, Na, K, V ⁇ Mg, A Ca,! / 2 Sr, V 2 Ba, or thallium.
  • an (earth) alkali metal such as Li, Na, K, V ⁇ Mg, A Ca,! / 2 Sr, V 2 Ba, or thallium.
  • Solvents for the production process are aprotic, polar or non-polar solvents, such as aliphatic and aromatic hydrocarbons or aliphatic and aromatic halogenated hydrocarbons.
  • aprotic solvents as are known to the person skilled in the art are also possible, but because of the simpler work-up, those with boiling points which are too high are less preferred.
  • Typical examples are n-hexane, cyclohexane, pentane, heptane, petroleum ether, toluene, benzene, chlorobenzene, methylene chloride, diethyl ether, tetrahydrofuran, ethylene glycol dimethyl ether.
  • the starting materials of the formulas (II), (III), (IV) and (V) can be prepared according to methods known in the literature or analogously to these.
  • the commercially available trimethylsilylcyclopentadiene can first be reacted with butyl lithium and then with trimethylsilyl chloride to give bis (trimethylsilyl) cyclopentadiene. This in turn can be done with
  • dimethylstannyldiphenylphosphine indenes by reacting indenes first with butyl lithium, as already mentioned above, and then with chlorodiphenylphosphine; the further reaction, first again with butyl lithium and then with chloro-tributyl tin gives the compound mentioned, which after further reaction with zirconium tetrachloride
  • Diphenylphosphino-indenyl-zirconium trichloride as a representative of compounds of formula (IV).
  • Such syntheses and methods of preparation are familiar to the person skilled in the field of organometallic and organochemical chemistry and have been published in numerous references, only a few of which have been mentioned above by way of example.
  • Cocatalyst is 1 to 100,000 mol cocatalyst per mol metallocene or ⁇ -complex compound.
  • Cocatalysts are, for example, aluminoxane compounds. Below are those of the formula
  • R represents C1-C20-alkyl, Cg-C ⁇ aryl or benzyl and n is a number from 2 to 50, preferably 10 to 35
  • Water can also be supplied as the (residual) moisture of the polymerization medium, the monomer or a carrier such as silica gel
  • bonds protruding from the square brackets of formula (XI) contain R groups or A1R2 groups as end groups of the oligomeric aluminoxane
  • aluminoxanes are present as a mixture of several of them with different chain lengths.
  • the detailed examination has also revealed aluminoxanes with a ring-shaped or cage-like structure.
  • Aluminoxanes are compounds which are commercially available.
  • cocatalysts are aluminum alkyls, lithium alkyls or Mg organic compounds, such as Grignard compounds or partially hydrolyzed boroganyls.
  • Preferred cocatalysts are aluminoxanes
  • the activation with the cocatalyst or the generation of the voluminous non- or weakly coordinating anion can be carried out in the autoclave or in a separate reaction vessel (preforming).
  • the activation can take place in the presence or absence of the monomer (s) to be polymerized.
  • the activation can be carried out in an aliphatic or aromatic or halogenated solvent or suspension medium
  • the ⁇ -complex compounds or metallocene compounds and the aluminoxanes can be used as such in homogeneous form or individually or together in heterogeneous form on carriers.
  • the carrier material can be inorganic or organic in nature, such as silica gel, Al2O3, MgCl2, NaCl , Cellulose derivatives, starches and polymers
  • the ⁇ -complex Compound or metallocene compound and first the aluminoxane are placed on the support and the other component is then added.
  • the metallocene compound can also be activated in a homogeneous or heterogeneous form with the aluminoxane and then the activated metallocene compound can be activated Bring carriers
  • Carrier materials are preferably thermally and / or chemically pretreated in order to adjust the water content or the OH group concentration in a defined manner or to keep them as med.
  • Chemical pretreatment can consist, for example, in the implementation of the carrier with aluminum alkyl.
  • Inorganic carriers are usually at 100 ° C. before use heated to 1000 ° C for 1 to 100 hours
  • the surface of such inorganic supports, in particular Sihca (SiO 2 ) is between 10 and 1000 m 2 / g, preferably between 100 and 800 m 2 / g.
  • the particle diameter is between 0 , 1 and 500 micrometers ( ⁇ ), preferably between 10 and 200 ⁇
  • Cyclic monomers are mono- or polycycic and fall under one of the two formulas
  • n is a number from 2 to 10, preferably 3 to 6,
  • Such cyclic monomers have one or more, preferably one or two, double bonds and are known, for example in the processes of EP-A
  • Preferred cyclic monomers of the formula (XV) are those of the formulas
  • cyclic comonomers include cyclobutene, cyclopentene, cyclopentadiene, cyclohexene, cycloheptene, cyclooctene, cyclodecene, cyclododecene, bicyclo-2-heptene, tricyclo-3-decene, tricyclo-3-undecene, tetracyclo dodecenes, pentacyclo-4-pentadecenes, pentacyclopentadecadienes, pentacyclo-3-pentadecenes, pentacyclo-4-hexadecenes, pentacyclo-3-hexadecenes, hexa- _ _
  • cyclo-4-heptadecenes heptacyclo-5-e ⁇ cocenes, heptacyclo-4-e ⁇ cocenes, heptacyclo-5-heneicocenes, octacyclo-5-dococenes, nonacyclo-5-pentacosenes, nonacyclo-6-hexacosenes, cyclopentadiene / acenaphthylene add 4-methano-l 4 4a 9a-tetrahydrofluorene and 1,4-methano-l 44a 5 10 lOa-hexahydroanthracene, such as, for example, b ⁇ cyclo [2,2, l] -hept-2-ene (norbornene), norbornadiene, 5- Methyl-norbornene, 6-methyl-norbornene, 5,6-dimethyl-norbornene, 1-methyl-norbornene, 5-isobutyl-
  • cycloolefins are also those formed by halogen, -CF 3 , -N (-CC 30 alkyl) 2 -CN, -C-C ] 2 alkoxy or are preferably substituted one to three times per molecule.
  • the cycloolefins can also be polymerized in the presence of acyclic mono- or diolefins, alkynes and carbon monoxide.
  • Suitable acyclic olefins include C 2 -C 4o-ct olefins and C 4 -C 2 4 diolefins such as ethylene, propylene, 1-butene, 1-pentene, 1-hexene, 3-methyl-1-butene, 3- Methyl-1-pentene, 4-methyl-1-pentene, 4-methyl-1-hexene, 4,4-dimethyl-1-hexene, 4,4-dimethyl-1-pentene, 4-ethyl-1-hexene, 3-ethyl-l-hexene, 1-octene, 1-
  • Decene 1-dodecene, 1-tetradecene, 1-hexadecene, 1-octadecene, 1-eicosen and mixtures of these ⁇ -olefins as well as 1,3-butadiene, isoprene, 1,3-pentadiene, 1, 4-hexadiene, 1, 4-hexadiene, 1,6-heptadiene, 1,6- and 1,7-octadiene, 1,8-nonadiene, 1,9-decadiene, 1,11-dodecadiene, 1,19-eicodiene and mixtures of these diolefins. Also mixtures of ⁇ -olefins and diolefins are suitable.
  • Such olefins and diolefins can also be substituted, for example with phenyl, substituted phenyl, halogen, the esterified carboxyl group, the acid anhydride group;
  • Compounds of this type are, for example, chloroprene, styrene, methylstyrene, chlorostyrene, fluorostyrene, indene, 4-vinylbiphenyl, vinylfluorene, vinylanthracene,
  • ring-opening polyadditions according to the invention for example of lactones, such as ⁇ -caprolactone or ⁇ -valerolactone, or of lactams, such as ⁇ -caprolactam, are possible.
  • Preferred monomers are: ethylene, propylene,
  • the cyclic monomer of the formulas (XIV) and (XV) represents a molar fraction of 1 to 100% of the total mol number of all comonomers used.
  • the ⁇ -olefin represents a molar fraction of 99 to 0% of the total mol number of all comonomers used.
  • the preferred amounts of Cycloolefin to ⁇ -olefin are 20 80 mol% to 80 20 mol%. In the event that cycloolefins of both the formula (XIV) and the formula (XV) are used, their molar ratio is 10 90 mol% to 90.10 mol%.
  • the process according to the invention is carried out at the temperatures and pressures indicated above in the gas, bulk, liquid or slurry phase, depending on whether a soluble or an insoluble catalyst of the type described above is used.
  • the liquid phase or the slurry phase can be formed from the comonomers alone, i.e. without the use of an additional solvent. If a solvent is also used, inert solvents, for example aliphatic or cycloaliphatic hydrocarbons, are used for this.
  • Chlorobenzene, o-dichlorobenzene or chloronaphthalene in question in the case of solvents with a low boiling point, the liquid phase can be maintained by applying a sufficient reaction pressure, these relationships being known to the person skilled in the art.
  • the polymers can be precipitated or reprecipitated by nonsolvents such as methanol and then dried
  • Such (co) polymerizations are known and familiar to the person skilled in the art. It is an advantage of the ⁇ -complex compounds or metallocene compounds according to the invention that by selecting the substituents they can be prepared both as soluble ⁇ -complex compounds or as insoluble ⁇ -complex compounds or metallocene compounds -Complex compounds or metallocene compounds, for example, will be used for the solution process, heterogeneous metallocene compounds, for example, will be used in the gas phase. According to the invention, batch or preferably continuous operation can be carried out using one or more reactors or reaction zones Different polymerization conditions can be set for several reactors or reaction zones
  • the ⁇ -complex compounds to be used according to the invention enable a defined opening of the two cyclopentadienyl skeletons in the manner of a beak through the donor-acceptor bridge, in addition to high activity, controlled selectivity, controlled molecular weight distribution and uniformity Installation of comonomers are guaranteed.
  • As a result of a defined beak-like opening there is also space for voluminous monomers.
  • the high uniformity in the molecular weight distribution is furthermore made possible from the uniform and defined location of the polymerization carried out by insertion (insertion) (single site catalyst) and can be adjusted by the choice of the polymerization temperature
  • the molecular weight distribution can be changed (broadened) in a targeted manner by using several D / A catalysts at the same time in order to set a specific material property profile. Accordingly, it is also possible to use one or more D / A catalysts in combination with other metallocenes that do not have any D / A Have A bridge
  • the D / A structure can bring about an extra stabilization of the catalysts up to high temperatures, so that the catalysts can also be used in the high temperature range.
  • the possible thermal dissociation of the donor-acceptor bond is reversible and leads through this self-assembly Process and
  • D / A metallocene compounds have the possibility of self-activation and thus dispense with expensive cocatalysts, in particular in the case of dianionic XX derivatives
  • the acceptor atom A in the opened form of the D / A- ⁇ complex compounds for example D / A-metallocene compound, binds an X ligand, for example one side of a dianion, with the formation of a zwitterionic metallocene structure and thus generates the Transition metal a positive charge, while the acceptor atom A assumes a negative charge.
  • Such self-activation can take place intramolecularly or intermolecularly. This is illustrated using the example of the preferred linkage of two X ligands to form a chelate ligand, namely the butadiene diyl derivative:
  • the binding site between the transition metal M and H or substituted or unsubstituted C, in the formula example the still bonded substituted C of the butadiene diyl dianion shown, is then the place for the olefin insertion for the polymerization.

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Abstract

Il est possible de fabriquer des copolymères de cyclo-oléfines, destinés à des mémoires de données optiques, par copolymérisation de monomères appartenant au groupe des oléfines cycliques, des α-oléfines comportant 2 atomes de carbone ou davantage, et des dioléfines éventuellement conjuguées ou non conjuguées, en utilisant comme catalyseurs des composés métallocènes ou des composés contenant le complexe π, de formules (I) ou (XIII), dans lesquelles CpI et CpII représentent des carbanions avec une structure contenant un cyclopentadiényle; πI et πII représentent des systèmes π chargés ou électriquement neutres; D représente un atome donneur et A un atome accepteur, D et A étant reliés par une liaison dative réversible, de façon que le groupe donneur devienne porteur d'une charge (partielle) positive et le groupe accepteur d'une charge (partielle) négative; M représente un métal de transition appartenant aux sous-groupes III, IV, V ou VI de la classification périodique des éléments (tableau de Mendeleïev), y compris les lanthanides et les actinides; X représente un équivalent anionique; et n est 0, 1, 2, 3 ou 4 en fonction de la charge de M.
PCT/EP1997/003459 1996-07-05 1997-07-02 Procede pour fabriquer des (co)polymeres de cyclo-olefines destines a des memoires de donnees optiques WO1998001483A1 (fr)

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JP10504738A JP2000514116A (ja) 1996-07-05 1997-07-02 光データメモリに使用するためのシクロオレフィン（コ）ポリマーの製造法
DE59702429T DE59702429D1 (de) 1996-07-05 1997-07-02 Verfahren zur herstellung von cycloolefin-(co)polymeren zur anwendung für optische datenspeicher
AU36927/97A AU3692797A (en) 1996-07-05 1997-07-02 Method for producing cycloolefin (co)polymers for use in optical data memories
AT97933647T ATE196771T1 (de) 1996-07-05 1997-07-02 Verfahren zur herstellung von cycloolefin- (co)polymeren zur anwendung für optische datenspeicher
EP97933647A EP0909285B1 (fr) 1996-07-05 1997-07-02 Procede pour fabriquer des (co)polymeres de cyclo-olefines destines a des memoires de donnees optiques
US09/214,206 US6232413B1 (en) 1996-07-05 1997-07-02 Method for producing cycloolefin (CO) polymers for use in optical data memories
NO990015A NO990015L (no) 1996-07-05 1999-01-04 FremgangsmÕte for fremstilling av cyklofelin (CO) polymerer for anvendelse i optisk dataminne

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
DE19627064A DE19627064C2 (de) 1996-07-05 1996-07-05 Metallocen-Verbindungen, Verfahren zu deren Herstellung, sowie ihre Verwendung
DE19627064.2 1996-07-05
DE19714058A DE19714058A1 (de) 1997-04-05 1997-04-05 pi-Komplex-Verbindungen
DE19714058.0 1997-04-05

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WO1998001483A1 true WO1998001483A1 (fr) 1998-01-15
WO1998001483A9 WO1998001483A9 (fr) 1998-05-14

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PCT/EP1997/003464 WO1998001487A1 (fr) 1996-07-05 1997-07-02 Procede pour fabriquer des elastomeres
PCT/EP1997/003461 WO1998001485A1 (fr) 1996-07-05 1997-07-02 Procede pour produire des polyolefines a point de fusion eleve
PCT/EP1997/003460 WO1998001484A1 (fr) 1996-06-05 1997-07-02 Procede pour fabriquer des (co)polymeres de cyclo-olefines destines a des applications techniques
PCT/EP1997/003462 WO1998001486A1 (fr) 1996-07-05 1997-07-02 Procede pour fabriquer des elastomeres thermoplastiques
PCT/EP1997/003459 WO1998001483A1 (fr) 1996-07-05 1997-07-02 Procede pour fabriquer des (co)polymeres de cyclo-olefines destines a des memoires de donnees optiques

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PCT/EP1997/003464 WO1998001487A1 (fr) 1996-07-05 1997-07-02 Procede pour fabriquer des elastomeres
PCT/EP1997/003461 WO1998001485A1 (fr) 1996-07-05 1997-07-02 Procede pour produire des polyolefines a point de fusion eleve
PCT/EP1997/003460 WO1998001484A1 (fr) 1996-06-05 1997-07-02 Procede pour fabriquer des (co)polymeres de cyclo-olefines destines a des applications techniques
PCT/EP1997/003462 WO1998001486A1 (fr) 1996-07-05 1997-07-02 Procede pour fabriquer des elastomeres thermoplastiques

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EP (5) EP0909281B1 (fr)
JP (5) JP2000514117A (fr)
KR (1) KR20000022453A (fr)
CN (5) CN1229417A (fr)
AT (5) ATE190632T1 (fr)
AU (5) AU3441597A (fr)
CA (5) CA2259553A1 (fr)
DE (5) DE59701094D1 (fr)
ES (5) ES2146106T3 (fr)
NO (5) NO985860L (fr)
RU (3) RU2203290C2 (fr)
WO (5) WO1998001487A1 (fr)

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DE19850898A1 (de) * 1998-11-05 2000-05-11 Bayer Ag Verfahren zur Herstellung von EP(D)M
DE19915108A1 (de) * 1999-04-01 2000-10-05 Bayer Ag Geträgerte Katalysatoren mit einer Donor-Akzeptor-Wechselwirkung
US6353064B1 (en) 1999-04-01 2002-03-05 Bayer Aktiengesellschaft Supported catalysts with a donor-acceptor interaction
US6657027B2 (en) 2001-03-23 2003-12-02 Bayer Aktiengesellschaft Catalysts with a donor-acceptor interaction
US7008569B2 (en) * 2001-04-27 2006-03-07 Jsr Corporation Thermoplastic norbornene resin based optical film
US7101496B2 (en) * 2001-04-27 2006-09-05 Jsr Corporation Thermoplastic norbornene resin based optical film
US7101498B2 (en) * 2001-12-25 2006-09-05 Jsr Corporation Thermoplastic norbornene resin based optical film
WO2004029065A1 (fr) * 2002-09-23 2004-04-08 Lanxess Deutschland Gmbh Composes a base de metal de transition presentant une interaction donneur-accepteur et un modele de substitution specifique

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US6191241B1 (en) 2001-02-20
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ATE190632T1 (de) 2000-04-15
EP0909282A1 (fr) 1999-04-21
CA2259434A1 (fr) 1998-01-15
NO318242B1 (no) 2005-02-21
EP0909285A1 (fr) 1999-04-21
JP2000514117A (ja) 2000-10-24
CA2259435A1 (fr) 1998-01-15
RU2203288C2 (ru) 2003-04-27
WO1998001485A1 (fr) 1998-01-15
ATE196771T1 (de) 2000-10-15
CN1229418A (zh) 1999-09-22
JP2000514116A (ja) 2000-10-24
CN1229416A (zh) 1999-09-22
ES2151740T3 (es) 2001-01-01
CN1097060C (zh) 2002-12-25
NO990015L (no) 1999-01-04
CN1100799C (zh) 2003-02-05
NO990014D0 (no) 1999-01-04
EP0909284B1 (fr) 2000-02-02
RU2203290C2 (ru) 2003-04-27
ATE189465T1 (de) 2000-02-15
EP0909281A1 (fr) 1999-04-21
NO990017L (no) 1999-02-15
CA2259435C (fr) 2006-01-24
NO985860L (no) 1999-02-15
US6172169B1 (en) 2001-01-09
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NO990013L (no) 1999-03-02
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US6156857A (en) 2000-12-05
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CN1097059C (zh) 2002-12-25
DE59701657D1 (de) 2000-06-15
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ES2146103T3 (es) 2000-07-16
ATE192755T1 (de) 2000-05-15
ATE192756T1 (de) 2000-05-15
CA2259553A1 (fr) 1998-01-15
CN1105118C (zh) 2003-04-09
NO319759B1 (no) 2005-09-12
RU2205189C2 (ru) 2003-05-27
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AU3441497A (en) 1998-02-02
CN1229415A (zh) 1999-09-22
WO1998001484A1 (fr) 1998-01-15
ES2144871T3 (es) 2000-06-16
AU3345697A (en) 1998-02-02
NO985860D0 (no) 1998-12-14
CA2259422A1 (fr) 1998-01-15
CA2259438C (fr) 2006-01-24
EP0909283A1 (fr) 1999-04-21
EP0909285B1 (fr) 2000-10-04
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US6174974B1 (en) 2001-01-16
WO1998001486A1 (fr) 1998-01-15
NO990017D0 (no) 1999-01-04
US6232413B1 (en) 2001-05-15
CA2259438A1 (fr) 1998-01-15
AU3692797A (en) 1998-02-02
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JP2000514120A (ja) 2000-10-24
AU3441697A (en) 1998-02-02
NO990013D0 (no) 1999-01-04
JP2000514119A (ja) 2000-10-24
EP0909283B1 (fr) 2000-03-15
DE59701656D1 (de) 2000-06-15
EP0909282B1 (fr) 2000-05-10
WO1998001487A1 (fr) 1998-01-15

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